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Human Genomics|May 14, 2026
Differences in miRNAs profile in pregnant women with preeclampsia compared with healthy pregnant womenVorapong Phupong, Natthaya Chuaypen, Supawadee Mingmongkol, et al.Human Genomics|February 27, 2026
Genetic variations in AAK1 and ADAM17 associated with circulatory cytokines changes influence COVID-19 susceptibility and severityAmal Bouzid, Noha M Elemam, Habiba Alsafar, et al.Human Genomics|March 11, 2026
Leveraging proteomics and machine learning for mechanism and biomarker discovery on glioma progression and transformation: from LGG to GBMQinhong Huang, Hui Liang, Jie Liu, et al.Human Genomics|February 25, 2026
Challenges in functional validation and mechanistic interpretation of a novel LACC1 variant in familial juvenile arthritisLin Yu, DuJiang Yang, Zhijun Ye, et al.Human Genomics|November 13, 2016
Novel genetic risk variants for pediatric celiac diseaseAngeliki Balasopoulou, Biljana Stanković, Angeliki Panagiotara, et al.Human Genomics|November 2, 2018
Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean populationSanghoon Moon, Young Lee, Sungho Won, et al.Human Genomics|February 22, 2017
Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activityDanielle Carpenter, Laura M Mitchell, John A L ArmourHuman Genomics|September 29, 2016
An efficient method for protein function annotation based on multilayer protein networksBihai Zhao, Sai Hu, Xueyong Li, et al.Human Genomics|September 16, 2019
SLC39A8 gene encoding a metal ion transporter: discovery and bench to bedsideDaniel W Nebert, Zijuan LiuHuman Genomics|October 23, 2019
Using Apache Spark on genome assembly for scalable overlap-graph reductionAlexander J Paul, Dylan Lawrence, Myoungkyu Song, et al.Pageof 112